摘要 |
The invention refers to a novel process for the preparation of cetirizine of formula (I) as well as to novel {2-[4-( alpha -phenyl-p-chloro-benzyl)piperazin-1-yl]ethoxy}acetamides of formula II, wherein R1 and R2 represent, independently, a C1-4 alkyl group optionally substituted by a phenyl group, a C2-4 alkenyl group or a cyclohexyl group, or R1 and R2 form together with the adjacent nitrogen atom a morpholino group. According to the novel process, an acetamide of formula (II) is hydrolized, if desired in the presence of a phase transfer catalyst, to obtain cetirizine. |
申请人 |
EGIS GYOGYSZERGYAR RT.;REITER, JOZSEF;TRINKA, PETER;BARTHA, FERENC;SIMIG, GYULA;NAGY, KALMAN;VERECZKEYNE DONATH, GYOERGYI;NEMETH, NORBERT;CLEMENTIS, GYOERGY;TOEMPE, PETER;VAGO, PAL |
发明人 |
REITER, JOZSEF;TRINKA, PETER;BARTHA, FERENC;SIMIG, GYULA;NAGY, KALMAN;VERECZKEYNE DONATH, GYOERGYI;NEMETH, NORBERT;CLEMENTIS, GYOERGY;TOEMPE, PETER;VAGO, PAL |